dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

Phenotypic Abnormality (PA): Lacrimal duct stenosis

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term
(+ for parents, - for children)
HP term [HP ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + + + + + 10:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + + 9:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + + + 8:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + + + 7:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + + + 6:   Abnormality of the orbital region [HP:0000315] <4>(17|24) (19|5|4)
+ + + + + 5:   Abnormality of the ocular adnexa [HP:0032039] <2>(17|24) (19|5|4)
+ + + + 4:   Abnormal ocular adnexa morphology [HP:0030669] <6>(17|24) (19|5|4)
+ + + 3:   Abnormal nasolacrimal system morphology [HP:0000614] <5>(2|2) (2|1|1)
+ + 2:   Abnormal lacrimal duct morphology [HP:0011481] <5>(2|2) (2|0|1)
+ 1:   Nasolacrimal duct obstruction [HP:0000579] <3>(1|1) (1|0|1)
0:   Lacrimal duct stenosis [HP:0007678](0|0) (0|0|0)